 | | Friday, December 09, 2011 |  | | | |  |
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Partnerships 2012:
The Largest Yet Most Intimate Gathering of Clinical Decision Makers in the World
The world has radically changed in just the last few years and the trend is likely to continue at an exponential rate. Partnerships in Clinical Trials is changing with it. Partnerships has always been where business gets done and strategic partnership deals are inked, but in 2012 it is where the industry moves forward with answers. We've taken your most pressing challenges and translated them into the most provocative meeting agenda the industry has ever seen.
For more information, please visit the conference site: http://www.iirusa.com/cropartners/welcome-to-CROs.xml?registration=XP1700BSENL. | | 
Innovative Clinical Trial Design and Management
• Use detailed case studies of recent adaptive trials featuring companies including Merck, Pfizer, Novartis, GSK, Eli Lilly, and AstraZeneca.
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• Assess the logistics of adaptive trial implementations.
Click Here for More Information. |  | |  • Biotech Bay (Sunnyvale, California)
Pharmacyclics, Inc.
Clinical Trial Assistant
Ensure studies are completed, on time, within budget and in compliance with SOPs, FDA regulations and ICH/GCP guidelines. Set up CTMS system, as appropriate. Assist in preparation of documents including regulatory document templates, study binders, study communications and presentations.
• Genetown (Cambridge, Massachusetts)
Millennium: The Takeda Oncology Company
Global Medical Affairs (GMA) Clinical Research Manager I
Lead provides oversight and management of Investigator Initiated Studies (IIS) for one or more molecule (s), either in development or post approval, within the IIS Program. The IIS Program includes studies submitted from US academic institutions, NCI CTEP/COOP, and Ex-US Investigators and/or COOPs.
• Biotech Beach (San Diego, California)
Ardea Biosciences, Inc.
Clinical Trials Assistant
Will support the efforts of a Phase 1, 2 or 3 clinical operations team (special emphasis on Phase 1's). Responsibilities include, but are not limited to maintaining clinical master files, making investigator payments.
• BioCapital (Bethesda, Maryland)
Technical Resources International
Attorney/Clinical Trials Agreement Advisor
Will draft and negotiate Clinical Trial Agreements and other research agreements between the government client (National Institutes of Health) and industry collaborators (biologic and drug product manufacturers) and provide counsel on FDA laws and regulations, contracts, intellectual property, access to data, ownership of data and specimens, safety reporting, patient privacy, liability, indemnification, confidentiality, and human subject protection.
• Pharm Country (Wayne, Pennsylvania)
On Assignment Clinical Research
Clinical SAS Programmer
Provide statistical programming support and validation and help set specifications of anlysis datasets, pooled datasets, statistical tables, summaries, figures and listing for Phase II-IV clinical trials. Employ standardized programs where applicable.
• Get Noticed! Add your resume to the BioSpace Career Center!
• See more than 5,000 job postings in the BioSpace Career Center! | | 
BioSpace Life Science Career Fairs are the biotech industry's premier career events. Featuring well-respected employers from around the nation, our job fairs attract top candidates in the biotech, pharmaceutical, life science and medical device industries.
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Hot Company
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More Company Profiles | | 
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Editorial & Production Staff: Lana Ho, Maysa Darwish, Tammy Liu, Michelle Wong
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